Showing entry for Velopharyngeal Insufficiency



                               
General Disease Information
BXGD IdBXGD002983
Disease NameVelopharyngeal Insufficiency
Disease CUI IdC0042454
MeSH Codes C16   C07   C09  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases; Otorhinolaryngologic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0000152  
Human Phenotype Ontology TermAbnormality of head or neck
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations
The  disease-related  target proteins
Proteins
Uniport Id BXGT Id Protein Name Gene Status Protein Class
Uniport Id BXGT Id Protein name Gene Status Protein class
P02458 BXGT005879 Collagen alpha-1(II) chain 1280 reviewed
P0CG47 BXGT007467 Polyubiquitin-B 7314 reviewed Nucleic acid binding
P12830 BXGT007852 Cadherin-1 999 reviewed
P21964 BXGT008714 Catechol O-methyltransferase 1312 reviewed Enzyme
Q12959 BXGT013283 Disks large homolog 1 1739 reviewed Receptor
Q15223 BXGT013551 Nectin-1 5818 reviewed
Q96PY6 BXGT019712 Serine/threonine-protein kinase Nek1 4750 reviewed Kinase
Q9BUF5 BXGT020135 Tubulin beta-6 chain 84617 reviewed Cellular structure
The  disease-related  compounds
Compounds
BXGC Id Compound Name Structure Molecular Weight Number of targets?Number of times compound connecting the disease , higher numbers indicate the compound is more associated with the disease
The  disease-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compounds in food?Number of compounds in food that connecting disease, higher numbers indicate the more compounds in food are more associated with the dusease